Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs35449651
rs35449651
PPP1R3A
1 1.000 0.080 7 113878300 missense variant G/T snv 1.4E-03 1.5E-03 0.700 0
dbSNP: rs371977235
rs371977235
SLC2A2
1 1.000 0.080 3 171005284 splice donor variant C/T snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs387906779
rs387906779
MTNR1B
1 1.000 0.080 11 92969849 missense variant G/C snv 7.0E-06 0.700 0
dbSNP: rs587777732
rs587777732
HNF4A ; MIR3646
9 0.763 0.240 20 44406195 missense variant C/T snv 0.700 0
dbSNP: rs587780345
rs587780345
GCK ; LOC105375258
5 0.851 0.080 7 44150004 missense variant C/T snv 0.700 0
dbSNP: rs72559715
rs72559715
ABCC8
5 0.827 0.160 11 17394379 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs72559722
rs72559722
ABCC8
6 0.807 0.160 11 17412716 stop gained G/A snv 6.1E-05 2.1E-05 0.700 0
dbSNP: rs72559734
rs72559734
ABCC8
6 0.807 0.160 11 17474955 missense variant C/A;T snv 4.0E-06; 8.0E-06 0.700 0
dbSNP: rs754729248
rs754729248
HNF1A
6 0.807 0.280 12 120996568 missense variant C/A;G;T snv 2.4E-05; 1.9E-04; 3.6E-05 0.700 0
dbSNP: rs76474829
rs76474829
LOC105372630
1 1.000 0.080 20 45285365 intergenic variant C/G;T snv 0.700 0
dbSNP: rs769268803
rs769268803
GCK ; LOC105375258
4 0.851 0.080 7 44147747 missense variant C/G;T snv 4.0E-06 0.700 0
dbSNP: rs80356661
rs80356661
PDX1
3 0.882 0.120 13 27924341 missense variant G/T snv 0.700 0
dbSNP: rs948820149
rs948820149
PPARG
1 1.000 0.080 3 12350786 intron variant A/C;G snv 7.0E-06 0.700 0
dbSNP: rs7107217
rs7107217 		3 0.882 0.160 11 129603795 intron variant A/C;G snv 0.810 1.000 1 2012 2012
dbSNP: rs7656416
rs7656416
CTBP1-DT
1 1.000 0.080 4 1260747 intron variant C/T snv 9.5E-02 0.810 1.000 1 2012 2012
dbSNP: rs8090011
rs8090011
LAMA1
1 1.000 0.080 18 7068463 intron variant C/A;G snv 0.810 1.000 1 2012 2012
dbSNP: rs10190052
rs10190052 		1 1.000 0.080 2 646674 intergenic variant T/C snv 0.82 0.800 1.000 1 2014 2014
dbSNP: rs10203174
rs10203174
THADA
1 1.000 0.080 2 43462891 intron variant C/T snv 0.17 0.800 1.000 1 2012 2012
dbSNP: rs1048886
rs1048886
SDHAF4
1 1.000 0.080 6 70579486 missense variant A/G snv 0.18 0.22 0.800 1.000 1 2011 2011
dbSNP: rs10510110
rs10510110
PLEKHA1
2 0.925 0.120 10 122432914 3 prime UTR variant T/C snv 0.56 0.800 1.000 1 2014 2014
dbSNP: rs10814916
rs10814916
GLIS3
7 0.851 0.200 9 4293150 intron variant A/C snv 0.57 0.800 1.000 1 2013 2013
dbSNP: rs10830962
rs10830962 		7 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs11066453
rs11066453
OAS1
4 1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 0.800 1.000 1 2013 2013
dbSNP: rs12010175
rs12010175
CCNQ
1 1.000 0.080 X 153597180 intron variant A/G snv 0.800 1.000 1 2013 2013
dbSNP: rs12027542
rs12027542
PCNX2
1 1.000 0.080 1 233204408 intron variant A/G snv 6.6E-02 0.800 1.000 1 2011 2011